MIB-626 is under clinical development by Metro International Biotech and currently in Phase II for Coronavirus Disease 2019 (COVID-19). According to GlobalData, Phase II drugs for Coronavirus Disease 2019 (COVID-19) have a 76% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how MIB-626’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
MIB-626 overview
MIB-626 is under development for the treatment of coronavirus disease 2019 (COVID-19), acute renal failure (ARF) (acute kidney injury) and mild dementia. The drug candidate is a crystallized precursor of nicotinamide adenine dinucleotide (NAD+). It is administered through oral route.
It was also under development for the treatment of muscle endurance (musculoskeletal disorders), mitochondrial myopathy, Friedreich’s ataxia (FA), and Leber’s hereditary optic neuropathy.
Metro International Biotech overview
Metro International Biotech is a clinical-stage pharmaceutical company that develops nicotinamide adenine dinucleotide (NAD+) cellular protection mechanisms for mitochondrial diseases. Its NAD+ is a cofactor required for the enzymatic processes that generate energy within the cell through the adenosine triphosphate (ATP) cycle. Metro International Biotech also offers a solid oral dosage formulation of MIB-626. The company’s NAD+ serves in therapeutic areas for various aging and numerous diseases such as mitochondrial dysfunction, inflammation and other related diseases. Metro International Biotech is headquartered in Worcester, Massachusetts, the US.
For a complete picture of MIB-626’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
